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FRESENIUS ARTERIAL BLOODLINE SETS FOR HEMODIALYSIS, FRESENIUS COMBI SETS HEMODIALYSIS BLOOD TUBING SETS

Page Type
Cleared 510(K)
510(k) Number
K012242
510(k) Type
Special
Applicant
Fresenius Medical Care North America
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/2001
Days to Decision
30 days
Submission Type
Summary

FRESENIUS ARTERIAL BLOODLINE SETS FOR HEMODIALYSIS, FRESENIUS COMBI SETS HEMODIALYSIS BLOOD TUBING SETS

Page Type
Cleared 510(K)
510(k) Number
K012242
510(k) Type
Special
Applicant
Fresenius Medical Care North America
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/2001
Days to Decision
30 days
Submission Type
Summary